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Trestle Luxe 71731-02Recalls & reported problems

Alphatec Spine, Inc. · Inner Shaft, Hexalobe Screw Removal Tool · Class 1

All models of Trestle Luxe (24)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840967192673), received between Mar 16, 2020 and Mar 16, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Break1
  • Fracture1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 16, 2020Break; Fracture

    DURING AN ACDF CASE OF THE C4-C7, THE SURGEON WAS INSERTING SCREWS USING THE SCREW REMOVER TOOL AND THE DISTAL TIPS FRACTURED AND BROKE. THE TIPS OF BOTH THE OUTER AND INNER SHAFTS REMAIN WITHIN THE SCREW HEAD POSITIONED WITHIN THE RIGHT C5 VERTEBRAE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9835069 ↗

Other SCREWDRIVER devices

All SCREWDRIVER devices →

Sources and updates

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